Blood biomarkers on admission in acute traumatic brain injury: Relations to severity, CT findings and care path in the CENTER-TBI study

EBioMedicine. 2020 Jun:56:102785. doi: 10.1016/j.ebiom.2020.102785. Epub 2020 May 25.

Abstract

Background: Serum biomarkers may inform and improve care in traumatic brain injury (TBI). We aimed to correlate serum biomarkers with clinical severity, care path and imaging abnormalities in TBI, and explore their incremental value over clinical characteristics in predicting computed tomographic (CT) abnormalities.

Methods: We analyzed six serum biomarkers (S100B, NSE, GFAP, UCH-L1, NFL and t-tau) obtained <24 h post-injury from 2867 patients with any severity of TBI in the Collaborative European NeuroTrauma Effectiveness Research (CENTER-TBI) Core Study, a prospective, multicenter, cohort study. Univariable and multivariable logistic regression analyses were performed. Discrimination was assessed by the area under the receiver operating characteristic curve (AUC) with 95% confidence intervals.

Findings: All biomarkers scaled with clinical severity and care path (ER only, ward admission, or ICU), and with presence of CT abnormalities. GFAP achieved the highest discrimination for predicting CT abnormalities (AUC 0•89 [95%CI: 0•87-0•90]), with a 99% likelihood of better discriminating CT-positive patients than clinical characteristics used in contemporary decision rules. In patients with mild TBI, GFAP also showed incremental diagnostic value: discrimination increased from 0•84 [95%CI: 0•83-0•86] to 0•89 [95%CI: 0•87-0•90] when GFAP was included. Results were consistent across strata, and injury severity. Combinations of biomarkers did not improve discrimination compared to GFAP alone.

Interpretation: Currently available biomarkers reflect injury severity, and serum GFAP, measured within 24 h after injury, outperforms clinical characteristics in predicting CT abnormalities. Our results support the further development of serum GFAP assays towards implementation in clinical practice, for which robust clinical assay platforms are required.

Funding: CENTER-TBI study was supported by the European Union 7th Framework program (EC grant 602150).

Keywords: Biomarkers; Clinical decision rule; Computerized tomography; Diagnostic; GFAP; Injury severity; Serum; Traumatic brain injury.

Publication types

  • Clinical Trial
  • Multicenter Study

MeSH terms

  • Aged
  • Aged, 80 and over
  • Area Under Curve
  • Biomarkers / blood*
  • Brain Injuries, Traumatic / blood
  • Brain Injuries, Traumatic / diagnostic imaging*
  • Female
  • Glial Fibrillary Acidic Protein / blood*
  • Humans
  • Male
  • Neurofilament Proteins / blood
  • Patient Admission
  • Patient Care Planning
  • Prospective Studies
  • ROC Curve
  • S100 Calcium Binding Protein beta Subunit / blood
  • Severity of Illness Index
  • Tomography, X-Ray Computed / methods*
  • Ubiquitin Thiolesterase / blood
  • tau Proteins / blood

Substances

  • Biomarkers
  • GFAP protein, human
  • Glial Fibrillary Acidic Protein
  • MAPT protein, human
  • Neurofilament Proteins
  • S100 Calcium Binding Protein beta Subunit
  • S100B protein, human
  • UCHL1 protein, human
  • neurofilament protein L
  • tau Proteins
  • Ubiquitin Thiolesterase